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Published on: October 12, 2017
Pro-oxidant HDL predicts poor outcome in patients with ST-elevation acute coronary syndrome
Klaus Distelmaier, Lore Schrutka, Veronika Seidl
1Irene Lang, MD, Medical University of Vienna, Department of Internal Medicine II, Division of Cardiology, Waehringer Guertel 18-20, A-1090 Vienna, Austria, Tel.: +43 1 40400 46140, Fax: +43 1 40400 42160,
Insights
Pro-oxidant high-density lipoprotein (HDL) increases mortality risk in ST-elevation acute coronary syndrome (STE-ACS) patients. Elevated neutrophil counts predict this harmful HDL, suggesting HDL function maintenance as a therapeutic target.
Area of Science:
- Cardiology
- Biochemistry
- Clinical Medicine
Background:
- Oxidative stress impacts outcomes in ST-elevation acute coronary syndrome (STE-ACS).
- High-density lipoprotein (HDL) typically offers protection, but can exhibit detrimental properties in acute myocardial infarction.
- The pro-oxidant nature of HDL in STE-ACS patients requires further investigation regarding its association with mortality.
Purpose of the Study:
- To analyze the association between pro-oxidant HDL and all-cause mortality in patients with STE-ACS.
- To identify predictors of pro-oxidant HDL in this patient population.
Main Methods:
- Prospective enrollment of 247 STE-ACS patients undergoing primary percutaneous coronary intervention.
- Determination of HDL antioxidant function using a serum HDL oxidant index (HOI).
- Stratification of patients into pro-oxidant (HOI≥1) and antioxidant (HOI<1) HDL groups, with multivariate regression analysis for survival.
Main Results:
- Pro-oxidant HDL was present in 44.1% of STE-ACS patients.
- Pro-oxidant HDL was independently associated with all-cause mortality (HR 3.30, p=0.003).
- Higher mortality rates were observed in patients with pro-oxidant HDL at 30 days (11.9% vs 2.2%) and 4 years (22.9% vs 8.7%).
- Elevated neutrophil counts (OR 1.50), prior myocardial infarction, high triglycerides, and reduced GFR predicted pro-oxidant HDL.
Conclusions:
- Pro-oxidant HDL is a strong, independent predictor of short-term and long-term all-cause mortality in STE-ACS patients.
- Elevated neutrophil counts are a significant predictor of pro-oxidant HDL.
- Maintaining HDL function may represent a promising therapeutic strategy for STE-ACS patients.
Abstract:
Oxidative stress affects clinical outcome in patients with ST-elevation acute coronary syndrome (STE-ACS). Although high-density lipoprotein (HDL) particles are generally considered protective, deleterious properties of HDL have been observed in patients with acute myocardial infarction. Here, we analysed the association between pro-oxidant HDL and all-cause mortality in STE-ACS patients. We determined the antioxidant function of HDL in 247 prospectively enrolled patients undergoing primary percutaneous coronary intervention for STE-ACS. Patients were stratified as by a pro-oxidant serum HDL oxidant index (HOI≥ 1) or with an antioxidant serum HOI (HOL< 1) capacity. Multivariate regression analysis was used to relate HOI to survival. The median follow-up time was 23 months (IQR 14.4-40.0 months). Pro-oxidant HDL was observed in 44.1 % of STE-ACS patients and was independently associated with all-cause mortality with a hazard ratio of 3.30(95 %CI 1.50-7.27, p = 0.003). Mortality rates were higher in patients with baseline pro-oxidant HDL compared to patients with preserved HDL function at 30 days (11.9 % vs 2.2 %, p=0.002), and at 4 years (22.9 % vs 8.7 %, p=0.002). Elevated neutrophil counts were a strong and independent predictor for pro-oxidant HDL with an odds ratio per standard deviation of 1.50 (95 %CI 1.11-2.03, p=0.008), as was history of prior acute myocardial infarction, elevated triglycerides levels and reduced glomerular filtration rate. In conclusion, pro-oxidant HDL represents a strong and independent predictor of long-term as well as short-term all-cause mortality in STE-ACS patients. Elevated neutrophil counts predicted the presence of serum pro-oxidant HDL. The maintenance of HDL functions might be a promising therapeutic target in STE-ACS patients.
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